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N-[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[[2-[[2-[[6-[[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]amino]-6-oxohexyl]amino]-2-oxoethyl]-[2-[2-[2-[bis[2-[[6-[[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]amino]-6-oxohexyl]amino]-2-oxoethyl]amino]ethoxy]ethoxy]ethyl]amino]acetyl]amino]hexanamide | 1214718-92-9

中文名称
——
中文别名
——
英文名称
N-[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[[2-[[2-[[6-[[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]amino]-6-oxohexyl]amino]-2-oxoethyl]-[2-[2-[2-[bis[2-[[6-[[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]amino]-6-oxohexyl]amino]-2-oxoethyl]amino]ethoxy]ethoxy]ethyl]amino]acetyl]amino]hexanamide
英文别名
——
N-[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[[2-[[2-[[6-[[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]amino]-6-oxohexyl]amino]-2-oxoethyl]-[2-[2-[2-[bis[2-[[6-[[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]amino]-6-oxohexyl]amino]-2-oxoethyl]amino]ethoxy]ethoxy]ethyl]amino]acetyl]amino]hexanamide化学式
CAS
1214718-92-9
化学式
C70H124N14O30
mdl
——
分子量
1641.83
InChiKey
PZPAGUYXNKLDBA-YZMQBHCJSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    -9.9
  • 重原子数:
    114
  • 可旋转键数:
    53
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    654
  • 氢给体数:
    24
  • 氢受体数:
    32

反应信息

  • 作为产物:
    描述:
    乙二醇双(2-氨基乙基醚)四乙酸 、 N-1-(ε-aminocaproyl)-β-N-acetyl-2-deoxyglucopyranosyl 在 O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate 、 三乙胺N,N-二异丙基乙胺 作用下, 以 二甲基亚砜 为溶剂, 反应 72.5h, 以26%的产率得到N-[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[[2-[[2-[[6-[[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]amino]-6-oxohexyl]amino]-2-oxoethyl]-[2-[2-[2-[bis[2-[[6-[[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]amino]-6-oxohexyl]amino]-2-oxoethyl]amino]ethoxy]ethoxy]ethyl]amino]acetyl]amino]hexanamide
    参考文献:
    名称:
    Molecular design of N-linked tetravalent glycosides bearing N-acetylglucosamine, N,N′-diacetylchitobiose and N-acetyllactosamine: Analysis of cross-linking activities with WGA and ECA lectins
    摘要:
    Two types of nonspacer- and spacer-N-linked tetravalent glycosides bearing N-acetylglucosamine (GlcNAc), N,N'-diacetylchitobiose [(GlcNAc)(2)] and N-acetyllactosamine (LacNAc) were designed and prepared as glycomimetics. The interactions of wheat germ (Triticum vulgaris) agglutinin (WGA) and coral tree (Erythrina cristagalli) agglutinin (ECA) with a series of tetravalent glycosides and related compounds were studied using a hemagglutination inhibition assay, a precipitation assay, double-diffusion test, and an optical biosensor based on surface plasmon resonance (SPR). The tetravalent glycosides were found to be capable of binding and precipitating the lectins as tetravalent ligands. Strong interactions with WGA, due to a combination of multivalency effects and spacer effects, were observed for tetravalent glycosides bearing flexible tandem GlcNAc. The chelate effect leads to large rate enhancement for the tetravalent system with favorable orientation of ligands. Our simple strategy produced multivalent glycosides with strong cross-linking activity for lectin as a specific coagulant. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2009.12.006
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文献信息

  • Molecular design of N-linked tetravalent glycosides bearing N-acetylglucosamine, N,N′-diacetylchitobiose and N-acetyllactosamine: Analysis of cross-linking activities with WGA and ECA lectins
    作者:Ryuichi Masaka、Makoto Ogata、Yoshinori Misawa、Megumi Yano、Chika Hashimoto、Takeomi Murata、Hirokazu Kawagishi、Taichi Usui
    DOI:10.1016/j.bmc.2009.12.006
    日期:2010.1
    Two types of nonspacer- and spacer-N-linked tetravalent glycosides bearing N-acetylglucosamine (GlcNAc), N,N'-diacetylchitobiose [(GlcNAc)(2)] and N-acetyllactosamine (LacNAc) were designed and prepared as glycomimetics. The interactions of wheat germ (Triticum vulgaris) agglutinin (WGA) and coral tree (Erythrina cristagalli) agglutinin (ECA) with a series of tetravalent glycosides and related compounds were studied using a hemagglutination inhibition assay, a precipitation assay, double-diffusion test, and an optical biosensor based on surface plasmon resonance (SPR). The tetravalent glycosides were found to be capable of binding and precipitating the lectins as tetravalent ligands. Strong interactions with WGA, due to a combination of multivalency effects and spacer effects, were observed for tetravalent glycosides bearing flexible tandem GlcNAc. The chelate effect leads to large rate enhancement for the tetravalent system with favorable orientation of ligands. Our simple strategy produced multivalent glycosides with strong cross-linking activity for lectin as a specific coagulant. (C) 2009 Elsevier Ltd. All rights reserved.
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